510(k) K072155 ยท PDU Catheter For Crossing Total Occlusions
PIONEER CATHETER
| Applicant | Medtronic, Inc., Santa Rosa CA, US |
| Decision | Substantially Equivalent, Oct 5, 2007 |
| Received | Aug 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072155
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.